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Results 1 - 6 of 6 for "Hyperaldosteronism," "familial," type I
  1. Familial hyperaldosteronism 
    ... type III National Organization for Rare Disorders (NORD) HYPERALDOSTERONISM, FAMILIAL, TYPE I; HALD1 HYPERALDOSTERONISM, FAMILIAL, TYPE II; HALD2 HYPERALDOSTERONISM, ...
    https://medlineplus.gov/.../condition/familial-hyperaldosteronism - Genetics
  2. KCNJ5 gene 
    ... gene mutations have been identified in people with familial hyperaldosteronism type III. These mutations, known as germline mutations, are ... WE. a Novel Y152C KCNJ5 mutation responsible for familial hyperaldosteronism type III. J Clin Endocrinol Metab. 2013 Nov;98( ...
    https://medlineplus.gov/genetics/gene/kcnj5 - Genetics
  3. CYP11B1 gene 
    ... A genetic change affecting the CYP11B1 gene causes familial hyperaldosteronism type I, a disorder that leads to hypertension. This ... production, which leads to the hypertension associated with familial hyperaldosteronism type I. More About This Health Condition C11B1_HUMAN ...
    https://medlineplus.gov/genetics/gene/cyp11b1 - Genetics
  4. CYP11B2 gene 
    ... A genetic change affecting the CYP11B2 gene causes familial hyperaldosteronism type I, a disorder that leads to high blood ... production, which leads to the hypertension associated with familial hyperaldosteronism type I. More About This Health Condition Normal variations ( ...
    https://medlineplus.gov/genetics/gene/cyp11b2 - Genetics
  5. Hypertension 
    ... key feature of some rare genetic disorders, including familial hyperaldosteronism, pseudohypoaldosteronism type 2, Liddle syndrome, and tumors known as paragangliomas. ...
    https://medlineplus.gov/genetics/condition/hypertension - Genetics
  6. Autosomal dominant hypocalcemia 
    ... magnesium and a buildup of the hormone aldosterone (hyperaldosteronism) in the ... or Bartter syndrome type V.There are two types of autosomal dominant ...
    https://medlineplus.gov/.../autosomal-dominant-hypocalcemia - Genetics